1012886-58-6

Basic information

• Product Name: methyl 2-(2-methoxyphenyl)-2-((4-methoxyphenyl)amino)acetate
• Synonyms: methyl 2-(2-methoxyphenyl)-2-((4-methoxyphenyl)amino)acetate
• CAS NO: 1012886-58-6
• Molecular Weight: 301.342
• Mol File: 1012886-58-6.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: methyl 2-(2-methoxyphenyl)-2-((4-methoxyphenyl)amino)acetate(CAS DataBase Reference)
• NIST Chemistry Reference: methyl 2-(2-methoxyphenyl)-2-((4-methoxyphenyl)amino)acetate(1012886-58-6)
• EPA Substance Registry System: methyl 2-(2-methoxyphenyl)-2-((4-methoxyphenyl)amino)acetate(1012886-58-6)

Safety Data

• Hazardous Substances Data: 1012886-58-6(Hazardous Substances Data)

Upstream product

• 104-94-9 4-methoxy-aniline 
• 347187-58-0 methyl α-diazo-α-(2-methoxyphenyl)acetate 
• 958221-49-3 (E)-1-(2-methoxyphenyl)-N-(4-methoxyphenyl)methanimine 
• 61985-23-7 methyl 1-imidazolecarboxylate 

Relevant articles and documents

Nitrogen-Doped Carbon Enables Heterogeneous Asymmetric Insertion of Carbenoids into Amines Catalyzed by Rhodium Nanoparticles

Development of stable heterogeneous catalyst systems is a crucial subject to achieve sustainable society. Though metal nanoparticles are robust species, the study of asymmetric catalysis by them has been restricted because methods to activate metal nanopa

Electroreductive acylation of aromatic imines with acylimidazoles

The intermolecular reductive coupling of aromatic imines with acylimidazoles was effected by electroreduction in the presence of chlorotrimethylsilane and gave α-amino-α-aryl ketones. This method was also effective for the synthesis of α-amino-α-aryl esters using methoxycarbonylimidazole as an electrophile.